4.7 Article

Experimental re-infected cats do not transmit SARS-CoV-2

Journal

EMERGING MICROBES & INFECTIONS
Volume 10, Issue 1, Pages 638-650

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/22221751.2021.1902753

Keywords

SARS-CoV-2; COVID-19; re-infection; transmission; cats

Funding

  1. NBAF Transition Funds from the State of Kansas
  2. NIAID Centers of Excellence for Influenza Research and Surveillance [HHSN 272201400006C]
  3. National Institute of General Medical Sciences (NIGMS) of the National Institutes of Health [P20GM130448]
  4. Department of Homeland Security Center of Excellence for Emerging and Zoonotic Animal Diseases [HSHQDC 16-A-B0006]
  5. Louisiana State University, School of Veterinary Medicine start-up fund [PG 002165]
  6. US Department of Agriculture, Agricultural Research Service [58-32000-009-00D]
  7. Center for Research for Influenza Pathogenesis (CRIP), a NIAID [HHSN272201400008C]
  8. JPB Foundation
  9. Open Philanthropy Project [2020-215611 [5384]]

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Studies have shown that cats previously infected with SARS-CoV-2 can be experimentally re-infected with the virus, but the levels of shed virus are insufficient for transmission to co-housed naive cats. Infection with SARS-CoV-2 in cats induces immune responses that provide partial, non-sterilizing immune protection against re-infection.
SARS-CoV-2 is the causative agent of COVID-19 and responsible for the current global pandemic. We and others have previously demonstrated that cats are susceptible to SARS-CoV-2 infection and can efficiently transmit the virus to naive cats. Here, we address whether cats previously exposed to SARS-CoV-2 can be re-infected with SARS-CoV-2. In two independent studies, SARS-CoV-2-infected cats were re-challenged with SARS-CoV-2 at 21 days post primary challenge (DPC) and necropsies performed at 4, 7 and 14 days post-secondary challenge (DP2C). Sentinels were co-mingled with the re-challenged cats at 1 DP2C. Clinical signs were recorded, and nasal, oropharyngeal, and rectal swabs, blood, and serum were collected and tissues examined for histologic lesions. Viral RNA was transiently shed via the nasal, oropharyngeal and rectal cavities of the re-challenged cats. Viral RNA was detected in various tissues of re-challenged cats euthanized at 4 DP2C, mainly in the upper respiratory tract and lymphoid tissues, but less frequently and at lower levels in the lower respiratory tract when compared to primary SARS-CoV-2 challenged cats at 4 DPC. Viral RNA and antigen detected in the respiratory tract of the primary SARS-CoV-2 infected cats at early DPCs were absent in the re-challenged cats. Naive sentinels co-housed with the re-challenged cats did not shed virus or seroconvert. Together, our results indicate that cats previously infected with SARS-CoV-2 can be experimentally re-infected with SARS-CoV-2; however, the levels of virus shed was insufficient for transmission to co-housed naive sentinels. We conclude that SARS-CoV-2 infection in cats induces immune responses that provide partial, non-sterilizing immune protection against re-infection.

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